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rs62094879

From SNPedia

Orientationplus
Stabilizedplus
Make rs62094879(C;C)
Make rs62094879(C;T)
Make rs62094879(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position57829073
is asnp
is mentioned by
dbSNPrs62094879
dbSNP (classic)rs62094879
ClinGenrs62094879
ebirs62094879
HLIrs62094879
Exacrs62094879
Gnomadrs62094879
Varsomers62094879
LitVarrs62094879
Maprs62094879
PheGenIrs62094879
Biobankrs62094879
1000 genomesrs62094879
hgdprs62094879
ensemblrs62094879
geneviewrs62094879
scholarrs62094879
googlers62094879
pharmgkbrs62094879
gwascentralrs62094879
openSNPrs62094879
23andMers62094879
SNPshotrs62094879
SNPdbers62094879
MSV3drs62094879
GWAS Ctlgrs62094879
GMAF0.09826
Max Magnitude0
GWAS snp
PMID [PMID 23319000]
Trait Metabolite levels (MHPG)
Title Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.
Risk Allele T
P-val 6E-6
Odds Ratio .29 unit decrease